MedPath

Loving Kindness Meditation Among Adults 50 Years and Older

Not Applicable
Completed
Conditions
Loneliness
Registration Number
NCT05350449
Lead Sponsor
University of Nevada, Las Vegas
Brief Summary

The goal of this clinical trial is to test the feasibility and acceptability of loving-kindness meditation among adults 50 years and older. It will also examine the benefits of this intervention and compare the outcomes between two groups (intervention and wait-list control).

Detailed Description

The main aim of the research is to assess the feasibility and acceptability of the Loving-kindness meditation intervention among adults 50 years or older. It will also examine the intervention's preliminary impact on loneliness, self-compassion, cognitive function, and psychological well-being. The study will use a randomized controlled trial with waitlist control.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
59
Inclusion Criteria

• Adults 50 years or older living in Southern Nevada

Exclusion Criteria

• Cognitive or language barrier that would make it difficult to understand and sign the informed consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change in Lonelinessbaseline, immediately post-intervention, and week 4 and week 8 post intervention (follow-up periods).

A 3-item modified UCLA loneliness scale will be used to measure loneliness. The scores on this scale range from 3 to 9, the highest scores indicative of a higher level of loneliness. We will measure loneliness at baseline, post-intervention and 2 follow-up periods to measure the change in loneliness level because of the loving-kindness meditation intervention.

Change in Self-compassionbaseline, immediately post-intervention, and week 4 and week 8 post intervention.

A 12-item Self-compassion Short form Scale by Kirsten Neff will be used to measure self-compassion. The scores on this scale rages from 1-5. The highest scores are indicative of better self-compassion. We will measure self-compassion at baseline and post-intervention periods to measure the change in self-compassion because of the loving-kindness meditation intervention.

Secondary Outcome Measures
NameTimeMethod
Change in Anxietybaseline, immediately post-intervention, and week 4 and week 8 post intervention.

A 4-item PROMIS Emotional Distress: Anxiety Scale will be used to measure anxiety. The scores on this scale range from 4 to 20, the highest scores indicative of a higher feeling of anxiety. We will measure anxiety at baseline and post-intervention periods to measure the change in anxiety level because of the loving-kindness meditation intervention.

Change in Depressive Symptomsbaseline, immediately post-intervention, and week 4 and week 8 post intervention.

A 10-item Center for Epidemiologic Studies Short Depression Scale will be used to measure depressive symptoms. The scores on this scale range from 10 to 40, the highest scores indicative of a higher feeling of depression. We will measure depressive symptoms at baseline and post-intervention periods to measure the change in depressive symptoms because of the loving-kindness meditation intervention.

Trial Locations

Locations (1)

University of Nevada Las Vegas

🇺🇸

Las Vegas, Nevada, United States

University of Nevada Las Vegas
🇺🇸Las Vegas, Nevada, United States

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